A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861984



Internal ID15809254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83475299..83510153hg38UCSC Ensembl
Innerchr16:83508904..83543758hg19UCSC Ensembl
Innerchr16:82066405..82101259hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3834855
hg1934855
hg1834855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573397
Supporting Variants
Samples
Known GenesCDH13, MIR3182
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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